Laminates and packaging containers

ABSTRACT

A laminate has a core layer and a skin layer on either side of the core layer, wherein the skin layer is formed of a copolymer having a glass transition point of 85° C. or more and 115° C. or below and consisting of 2,6-naphthalene dicarboxylic acid or its lower alkyl ester, terephthalic acid or its lower alkyl ester and ethylene glycol or a polymer alloy having a glass transition point of 85° C. or more and 115° C. or below and consisting of polyethylene terephthalate and polyethylene-2,6-naphthalate. Thus, it can be used suitably as a packaging container for food and drink, such as jelly containers, which has flavor resistance and aroma retention sufficient not to be limited by types of flavor used for jelly or the like, excels in sealing properties with a lid body, can be hermetically sealed with an easy-peel transparent lid body, and is also superior in gas barrier properties, impact resistance, heat resistance, cost efficiency and transparency.

TECHNICAL FIELD

The present invention relates to a plastic laminate and a containerwhich is formed of it and used for food, drink or the like.

BACKGROUND ART

As a material for food packaging, plastic having improved heatresistance and the like is now being used increasingly. And,polyethylene-2,6-naphthalate (PEN), which is one type of polyesterresin, is particularly superior to polyethylene terephthalate (PET) inmechanical strength (Young's modulus, breaking strength), heatresistance (long-term heat stability, dimensional stability),ultraviolet shielding property (weather resistance), chemical properties(chemical resistance, gas barrier properties) and the like because ofinflexibility and planarity of its molecular chain, and has come intothe limelight in recent years. But, it has inferior heat-sealingproperties with a lid material. Specifically, it has poor heat-sealingproperties with an aluminum closure (aluminum foil lid material) whichhas a polyester based adhesive layer as the innermost layer and alsoinferior adhesive force depending on use conditions. And, because theforming conditions are different when the PEN resin is contained, itcannot be included in a recycling system of the PET resin and also hasthe same drawback as the multi-layered film view of recyclingefficiency. Besides, there were also problems of impact resistance andhigh cost.

The present inventors have proposed, as packing materials for food whichare free from the drawbacks of polyethylene-2,6-naphthalate (PEN), apolyester copolymer indicated by a general formula, HO—(COArCOORO)_(n)—H(n is 100 to 1000. But, Ar is 2,6-naphthalene group and phenylene group,and R is ethylene group and 1,4-cyclohexylene group.) (Japanese PatentApplication Laid-Open Publication No. Hei 8-113631) and a laminatedsheet made of a polymer alloy formed of a polyarylate resin and athermoplastic polyester resin (Japanese Patent Application Laid-OpenPublication No. Hei 11-34271).

The former copolymer excels in heat resistance, impact resistance,heat-sealing properties with a lid material, gas barrier properties andrecycling efficiency, but the copolymer has a problem of high cost whenit is used as a single-layer film for a food packaging container. And,the latter laminated sheet is superior in heat resistance, impactresistance and heat-sealing properties with a lid material butinsufficient in gas barrier properties, flavor resistance (flavor attackresistance) and aroma retention. For example, when it is used as a jellycontainer, it has a problem of being limited by used flavor.

It is an object of the present invention to remedy the problems of theprior art and to provide a transparent plastic laminated sheet which hassufficient flavor resistance and aroma retention and also excels in gasbarrier properties (oxygen barrier properties), impact resistance, heatresistance, sealing properties and cost efficiency.

And, its object is to provide a transparent plastic laminated sheetwhich excels in heat-sealing properties with a lid material andrecycling efficiency, has sufficient flavor resistance and aromaretention, and also excels in gas barrier properties (oxygen barrierproperties), impact resistance, heat resistance, cold-impact resistanceand cost efficiency.

Besides, its object is to provide a packaging container for food, drinkand the like, which is formed of the above-described plastic laminatedsheet.

DISCLOSURE OF THE INVENTION

A first laminate of the present invention is a laminate having a corelayer and a skin layer on either side of the core layer, wherein theskin layer is formed of a copolymer having a glass transition point of85° C. or more and 115° C. or below and consisting of 2,6-naphthalenedicarboxylic acid or its lower alkyl ester, terephthalic acid or itslower alkyl ester and ethylene glycol or a polymer alloy having a glasstransition point of 85° C. or more and 115° C. or below and consistingof polyethylene terephthalate and polyethylene-2,6-naphthalate.

A second laminate of the present invention is a laminate having a corelayer and a skin layer on either side of the core layer, wherein theskin layer is formed of a polyester copolymer which consists of2,6-naphthalene dicarboxylic acid or its lower alkyl ester, terephthalicacid or its lower alkyl ester, 1,4-cyclohexane dimethanol and ethyleneglycol.

Besides, a packaging container of the present invention is a packagingcontainer having a container body with an opening at the upper part,wherein the container body is formed of the above-described laminate.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a diagram showing one example of the shape of a container bodyof the present invention, (a) is a top view and (b) is a cross-sectionalview.

FIG. 2 is a diagram showing another example of the shape of a containerbody of the present invention, (a) is a top view, and (b) is across-sectional view.

BEST MODE FOR CARRYING OUT THE INVENTION

The present invention will be described in detail.

The glass transition point in the present invention indicates a valuedetermined from a transition point by raising a temperature (10° C./min)by a differential scanning calorimetric analyzer (DSC).

[First Laminate]

A first laminate is a laminate having a core layer and a skin layer oneither side of the core layer.

The skin layer is made of a copolymer having a glass transition point of85° C. or more and 115° C. or below and consisting of 2,6-naphthalenedicarboxylic acid or its lower alkyl ester, terephthalic acid or itslower alkyl ester and ethylene glycol or a polymer alloy having a glasstransition point of 85° C. or more and 115° C. or below and consistingof polyethylene terephthalate and polyethylene-2,6-naphthalate.

Here, the lower alkyl ester of 2,6-naphthalene dicarboxylic acid and thelower alkyl ester of terephthalic acid are desired to have the number ofcarbon atoms of 1 to 8, preferably 1 to 5, and may also be monoester inaddition to diester.

Examples of the lower alkyl ester of 2,6-naphthalene dicarboxylic acidare 2,6-dimethyl naphthalate, 2,6-diethyl naphthalate, 2,6-dipropylnaphthalate, 2,6-dibutyl naphthalate, 2,6-dipentyl naphthalate,2,6-dihexyl naphthalate, 2,6-diheptyl naphthalate, 2,6-dioctylnaphthalate, and the like. Among them, 2,6-dimethyl naphthalate,2,6-diethyl naphthalate, 2,6-dipropyl naphthalate, 2,6-dibutylnaphthalate and 2,6-dipentyl naphthalate are particularly preferable.

Examples of the lower alkyl ester of terephthalic acid are dimethylterephthalate, diethyl terephthalate, dipropyl terephthalate, dibutylterephthalate, dipentyl terephthalate, dihexyl terephthalate, diheptylterephthalate, dioctyl terephthalate, and the like. And, dimethylterephthalate, diethyl terephthalate, dipropyl terephthalate, dibutylterephthalate, dipentyl terephthalate are particularly desirable.

All the above-described copolymers and polymer alloys have a glasstransition point of 85° C. or more and 115° C. or below, and preferably90° C. or more and 110° C. or below. For that, it is preferable that2,6-naphthalene group and phenylene group are in a molar ratio(2,6-naphthalene group/phenylene group) of 30/70 to 92/8, and desirably40/60 to 80/20, and more desirably 50/50 to 80/20. When the molar ratioof 2,6-naphthalene group is higher than the above range, it is notdesirable in view of impact resistance and cost efficiency, and when itis lower than the above range, it is not desirable in view of heatresistance and gas barrier properties.

Specific examples of the first laminate will be described below, but itis to be noted that the first laminate is not limited to them.

Embodiment 1-1

Embodiment 1-1 is a laminate having a three-layered structure formed ofa core layer and a skin layer which is laminated on either side of thecore layer.

The core layer is formed of a polymer alloy which consists of aheat-resistant resin and a thermoplastic polyester resin and contains 50to 65 wt % of the heat-resistant resin (hereinafter simply referred toas the “heat-resistant resin”) having a glass transition point of 140°C. to 250° C. and an Izod impact test value of 80 J/m to 850 J/m whentested with a ⅛″ notch under conditions of 23° C. and a relativehumidity of 50%. It is not desirable if the heat-resistant resin contentis less than 50 wt % in view of heat resistance and, if it exceeds 65 wt%, it is not desirable in view of extrudability, moldability and costefficiency.

Here, the thermoplastic polyester resin is a resin other than theheat-resistant resins and preferably a linear polyethylene terephthalatehomopolymer which has an ethylene terephthalate unit or a butyleneterephthalate unit as a repeating unit respectively, but terephthalicacid may be partly replaced with phthalic acid, isophthalic acid,succinic acid, adipic acid, sebacic acid, docecane dicarboxylic acid,hexahydroterephthalic acid, 2,6-naphthalene dicarboxylic acid,2,5-dibromterephthalic acid, diphenyl dicarboxylic acid, trimelliticacid, pyromellitic acid, or the like. And, ethylene glycol may be partlyreplaced with propylene glycol, diethylene glycol, tetraethylene glycol,polyethylene glycol, polytetramethylene glycol, 1,6-hexanediol,trimethylene glycol, neopentyl glycol, p-xylene glycol, 1,6-cyclohexanedimethanol, bisphenol A, glycerin, pentaerythritol, trimethanol propane,trimethanol benzene, triethanol benzene, or the like. Among them, apolyethylene terephthalate resin (PET) is particularly desirable.

And, one having an intrinsic viscosity (determined from a viscosity ofthe solution measured at 25° C. in a mixture solution of 50 wt % ofphenol and 50 wt % of tetrachloroethane,) in a range of from 0.5 to 1.4is desirable, and it is more desirable in a range of 0.6 to 1.2. Whenthe intrinsic viscosity is less than 0.5, extrusion processability andcontainer moldability become poor, and the molded container tends tohave a degraded strength against drop and to become fragile. And, whenthe intrinsic viscosity exceeds 1.4, there are tendencies that the costbecomes high and, productivity of sheets become worse.

Then, the heat-resistant resin includes, for example, polyarylate resin(PAR), polycarbonate resin (PC), polysulfone, polyether ketone, and thelike, and the polyarylate resin (PAR) is particularly desirable. Thepolyarylate resin (PAR) is obtained from aromatic dicarboxylic acid orits functional derivative and dihydric phenol or its functionalderivative.

As the aromatic dicarboxylic acid, any type may be acceptable as long asit reacts with dihydric phenol to provide a satisfactory polymer and maybe used alone or as a mixture of two or more. Preferable aromaticdicarboxylic acid includes terephthalic acid and isophthalic acid, and amixture of them is particularly desirable in view of melt processabilityand overall performance. Such a mixture is desired to be terephthalicacid/isophthalic acid=9/1 to 1/9 (molar ratio), and more desirably 7/3to 3/7 (molar ratio) in view of a balance of melt processability andperformance.

And, specific examples of the dihydric phenol are2,2-bis(4-hydroxyphenyl)propane,2,2-bis(4-hydroxy-3,5-dibromophenyl)propane,2,2-bis(4-hydroxy-3,5-dichlorophenyl)propane, 4,4-dihydroxy diphenylsulfone, 4,4-dihydroxy diphenyl ether, 4,4-dihydroxy diphenyl sulfide,4,4-dihydroxydiphenyl ketone, 4,4-dihydroxy phenylmethane,2,2-bis(4-hydroxy-3,5-dimethylphenyl)propane,1,1-bis(4-hydroxyphenyl)ethane, 1,1-bis(4-hydroxyphenyl)cyclohexane,4,4-dihydroxydiphenyl, benzoquinone, and the like. They may be usedalone or as a mixture of two or more. The above dihydric phenol is parasubstituted, but another isomer may be used. As the dihydric phenol,ethylene glycol, propylene glycol or the like can be used. Among thedihydric phenols, the most typical one is2,2-bis(4-hydroxyphenyl)propane, which is generally called bisphenol Aand most desirable in view of total physical properties.

Therefore, the most desirable polyarylate resin (PAR) of the presentinvention is obtained from a mixture of terephthalic acid andisophthalic acid, or a mixture of their functional derivatives (but, amolar ratio of a terephthalic acid residue and an isophthalic acidresidue is 9/1 to 1/9, and particularly 7/3 to 3/7) and dihydric phenol,particularly bisphenol A or its functional derivative. Specific examplesinclude a resin obtained from bisphenol A, terephthalic dichloride andisophthalic dichloride, and its structural formula is expressed by thefollowing general formula (1).

And, it is preferable that the polyarylate resin (PAR) according to thepresent invention has the intrinsic viscosity in a range of 0.5 to 0.8,which is determined from a solution viscosity measured in a mixturesolution of 50 wt % of phenol and 50 wt % of tetrachloroethane at 25°C., namely a weight-average molecular weight in a range of approximately7,000 to 100,000, in view of the physical properties of the laminate,the extrusion processing characteristics when the laminate isco-extrusion molded, container moldability, and the like.

Thickness is not particularly limited but preferably 200 μm to 3000 μm.The ratio of respective layers in thickness is not particularly limited,but it is preferable that the skin layer is 10 to 40% of the whole, andthe core layer is 90 to 60% of the whole.

Embodiment 1-1 has flavor resistance and aroma retention sufficient notto be limited by types of flavor used for jelly or the like, excels insealing properties with a lid body and can be hermetically sealed withan easy-peel transparent lid body. It is also superior in gas barrierproperties (oxygen barrier properties), impact resistance, heatresistance, cost efficiency and transparency and can be used suitably asa packaging container for food and drink, such as jelly containers.

Embodiment 1-2

Embodiment 1-2 is a laminate having a five-layered structure consistingof a core layer, an intermediate layer laminated on either side of thecore layer and a skin layer laminated on the intermediate layer.

The core layer is formed of a amorphous resin which includes athermoplastic polyester resin as the main constituent. A crystallineresin is not desirable because whitening may occur when forming.

Here, the same thermoplastic polyester resin as described in connectionwith the core layer of Embodiment 1-1 is used. The above-described mainconstituent means 50 wt % or more, preferably 93 wt % or more, of thethermoplastic polyester resin.

Specifically, a polymer alloy consisting of 90 wt % to 40 wt % ofpolyethylene terephthalate (PET), 5 wt % to 30 wt % ofpolyethylene-2,6-naphthalate (PEN) and 5 wt % to 30 wt % of aheat-resistant resin can be used suitably. And, in a range not changingthe molar ratio of 2,6-naphthalene group and phenylene group(2,6-naphthalene group/phenylene group), polyethylene terephthalate(PET) and polyethylene-2,6-naphthalate (PEN) may be replaced partly orwholly with a copolymer consisting of 2,6-naphthalene dicarboxylic acidor its lower alkyl ester, terephthalic acid or its lower alkyl ester andethylene glycol, or a returned item (skeleton: a residue remained bypunching a sheet to form a product such as a cup-shaped container or thelike) may be used.

The intermediate layer is formed of a polymer alloy consisting of aheat-resistant resin and a thermoplastic polyester resin, which contains50 to 65 wt % of the heat-resistant resin, and the same polymer alloy asthat forming the core layer of Embodiment 1-1 can be used.

Thickness is not particularly limited but desirably 200 μm to 3000 μm.And, the ratio of respective layers in thickness is not particularlylimited, but it is preferable that the skin layer is 10 to 45% of thewhole, the intermediate layer is 10 to 45% of the whole, and the corelayer is 80 to 10% of the whole, and it is more preferable that the skinlayer is 10 to 30% of the whole, the intermediate layer is 20 to 40% ofthe whole, and the core layer is 70 to 30% of the whole.

Embodiment 1-2 maintains the same effect as Embodiment 1-1 and can alsouse as a resin for the core layer a returned item, which is produced atthe time of sheet forming and container forming and superior in the costperformance.

Embodiment 1-3

Embodiment 1-3 is a laminate having a three-layered structure consistingof a core layer and a skin layer laminated on either side of the corelayer.

The core layer is formed of a copolymer having a glass transition pointof 110° C. or more and consisting of 2,6-naphthalene dicarboxylic acidor its lower alkyl ester, terephthalic acid or its lower alkyl ester andethylene glycol or a polymer alloy having a glass transition point of110° C. or more and consisting of polyethylene terephthalate andpolyethylene-2,6-naphthalate, and preferably having a different glasstransition point from the copolymer or the polymer alloy forming theskin layer.

Here, the lower alkyl ester of 2,6-naphthalene dicarboxylic acid and thelower alkyl ester of terephthalic acid can be the same as thosedescribed in connection with the skin layer.

The above copolymer and polymer alloy each have a glass transition pointof 110° C. or more, and preferably 115% or more. For that, a molar ratioof 2,6-naphthalene group and phenylene group (2,6-naphthalenegroup/phenylene group) is preferably 80/20 to 100/0, and more preferably92/8 to 100/0. When the molar ratio of the 2,6-naphthalene group islower than the above range, it is not desirable in view of oxygenbarrier properties and heat resistance.

Thickness is not particularly limited but desirably 200 μm to 3000 μm.And, the ratio of respective layers in thickness is not particularlylimited, but it is preferable that the skin layer is 10 to 40% of thewhole, and the core layer is 90 to 60% of the whole.

Embodiment 1-3 maintains the same effect as Embodiment 1-1, and itsoxygen barrier properties are better than Embodiment 1-1.

Embodiment 1-4

Embodiment 1-4 is a laminate having a five-layered structure consistingof a core layer, an intermediate layer laminated on either side of thecore layer and a skin layer laminated on the intermediate layer.

The core layer is formed of a amorphous resin including a thermoplasticpolyester resin as the main constituent. A crystalline resin is notdesirable because whitening may occur when forming.

Here, as the thermoplastic polyester resin, the same one as described inconnection with the core layer of Embodiment 1-1 is used. Theabove-described main constituent means 50 wt % or more, and desirably 93wt % or more, of the thermoplastic polyester resin.

Specifically, a polymer alloy consisting of 95 wt % to 60 wt % ofpolyethylene terephthalate (PET) and 5 wt % to 40 wt % ofpolyethylene-2,6-naphthalate (PEN) can be used suitably, and in a rangenot changing a molar ratio of 2,6-naphthalene group and phenylene group(2,6-naphthalene group/phenylene group), polyethylene terephthalate(PET) and polyethylene-2,6-naphthalate (PEN) may be partly or whollyreplaced with a copolymer consisting of 2,6-naphthalene dicarboxylicacid or its lower alkyl ester, terephthalic acid or its lower alkylester and ethylene glycol, or a returned item may be used.

The intermediate layer is formed of a copolymer having a glasstransition point of 110° C. or more and consisting of 2,6-naphthalenedicarboxylic acid or its lower alkyl ester, terephthalic acid or itslower alkyl ester and ethylene glycol or a polymer alloy having a glasstransition point of 110° C. or more and consisting of polyethyleneterephthalate and polyethylene-2,6-naphthalate, and the same copolymeror polymer alloy as that forming the core layer of Embodiment 1-3 can beused.

Thickness is not particularly limited but desirably 200 μm to 3000 μm.And, the ratio of respective layers in thickness is not particularlylimited, but it is preferable that the skin layer is 10 to 45% of thewhole, the intermediate layer is 10 to 45% of the whole, and the corelayer is 80 to 10% of the whole. And, it is more desirable that the skinlayer is 10 to 30% of the whole, the intermediate layer is 20 to 40% ofthe whole, and the core layer is 70 to 30% of the whole.

Embodiment 1-4 maintains the same effect as Embodiment 1-3, and areturned item can also be used as a resin for the core layer and issuperior in the cost performance.

Embodiment 1-5

Embodiment 1-5 is a laminate having a seven-layered structure consistingof a core layer, an intermediate layer laminated on either side of thecore layer and a skin layer laminated on the intermediate layer, whereinthe core layer consists of an innermost layer and an adhesive layerlaminated on either side of the innermost layer.

The innermost layer is formed of polyamide (MXD6) which is formed bymelt polymerization of a diamine component containing 70 mol % or moreof metaxylylene diamine and a dicarboxylic acid component containing 70mol % or more of adipic acid.

The diamine component is required to contain 70 mol % or more ofmetaxylylene diamine. When the diamine component contains 70% or more ofmetaxylylene diamine, remarkable gas barrier properties can bemaintained. The diamines usable other than metaxylylene diamine are, forexample, paraxylylene diamine, 1,3-bis(aminomethyl)cyclohexane,1,4-bis(aminomethyl)cyclohexane, tetramethylene diamine, hexamethylenediamine, nonamethylene diamine, 2-methyl-1,5-pentane diamine, and thelike.

And, the dicarboxylic acid component is required to contain 70 mol % ormore of adipic acid. When the dicarboxylic acid component contains 70mol % or more of adipic acid, it is possible to avoid degrading the gasbarrier properties and crystallizability. The dicarboxylic acidcomponents usable other than the adipic acid are, for example, subericacid, azelaic acid, sebacic acid, 1,10-decandicarboxylic acid,terephthalic acid, isophthalic acid, 2,6-naphthalene dicarboxylic acid,and the like.

As a molecular weight modifier, a small amount of monoamine ormonocarboxylic acid may be added at the time of polycondensation of thepolyamide.

The above polyamide is produced by a melt polycondensation process. Forexample, it is produced by a method which raises a temperature of nylonsalt consisting of adipic acid and metaxylylene diamine in the presenceof water under pressure and polymerizes in a molten state while removingthe added water and condensation water. It is also produced by directlyadding metaxylylene diamine to the adipic acid in a molten state andpolycondensing under ordinary pressure. In such a case, in order to keepthe reaction system in a uniform liquid state, metaxylylene diamine iscontinuously added to the adipic acid, during which the reaction systemis kept raised its temperature to prevent the reaction temperature fromlowering to a level lower than the melting points of oligoamide andpolyamide being produced so to proceed the polycondensation.

A relatively low-molecular-weight polyamide obtained by the meltpolymerization generally has relative viscosity of approximately 2.28 (avalue determined at 25° C. after dissolving 1 g of a polyamide resin in100 ml of a 96% aqueous sulfuric acid solution, and the same is alsoapplied below). When relative viscosity after the melt polymerization is2.28 or below, a gel-state substance is produced in a small amount, andpolyamide having high quality with good color tone can be obtained. Itis desirable that the relatively low-molecular-weight polyamide obtainedby the melt polymerization is further subjected to solid-statepolymerization. The solid-state polymerization is performed bypelletizing or powdering the relatively low-molecular-weight polyamideobtained by the melt polymerization and heating it to a temperature in arange of 150° C. to a melting point of the polyamide under reducedpressure or in an atmosphere of inert gas. The solid-state polymerizedpolyamide desirably has a relative viscosity of 2.3 to 4.2. In thisrange, the laminate or container can be formed favorably, and theobtained laminate or container has good performance, and particularlygood mechanical performance.

The adhesive layer is preferably an acid-modified polyolefin resin and,specifically, an “ADMER” produced by Mitsui Chemicals, “MODIC” producedby Mitsubishi Chemical Corporation, or the like can be used suitably.

The intermediate layer is formed of a polymer alloy consisting of aheat-resistant resin and a thermoplastic polyester resin, which contains50 to 65 wt % of the heat-resistant resin. And, the same polymer alloyas that forming the core layer of Embodiment 1-1 can be used.

Thickness is not particularly limited but desirably 200 μm to 3000 μm.And, the ratio of respective layers in thickness is not particularlylimited, but it is preferable that the skin layer is 10 to 82% of thewhole, the intermediate layer is 10 to 45% of the whole, the adhesivelayer is 3 to 20% of the whole, and the innermost layer is 5 to 25% ofthe whole.

Embodiment 1-5 maintains the same effect as Embodiment 1-1 and excelsEmbodiments 1-1 and 1-3 in oxygen barrier properties.

Embodiment 1-6

Embodiment 1-6 is a laminate having an eight-layered structure which hasan intermediate core layer formed between the intermediate layer and theadhesive layer on one side of the core layer in the laminated structureof Embodiment 1-5.

The intermediate core layer is formed of a amorphous resin whichincludes a thermoplastic polyester resin as the main constituent. Acrystalline resin is not desirable because whitening may occur at thetime of forming.

Here, the same thermoplastic polyester resin as that described inconnection with the core layer of Embodiment 1-1 can be used. Theabove-described main constituent means 50 wt % or more, and desirably 93wt % or more, of the thermoplastic polyester resin.

Specifically, a polymer alloy consisting of 20 wt % to 85 wt % ofpolyethylene terephthalate (PET), 2 wt % to 20 wt % ofpolyethylene-2,6-naphthalate (PEN), 5 wt % to 20 wt % of aheat-resistant resin, 4 wt % to 25 wt % of polyamide (MXD6) and 4 wt %to 15 wt % of an acid-modified polyolefin resin can be used suitably.And, in a range not changing the molar ratio of 2,6-naphthalene groupand phenylene group (2,6-naphthalene group/phenylene group),polyethylene terephthalate (PET) and polyethylene-2,6-naphthalate (PEN)may be partly or wholly replaced with a copolymer consisting of2,6-naphthalene dicarboxylic acid or its lower alkyl ester, terephthalicacid or its lower alkyl ester and ethylene glycol, or a returned itemmay be used.

Thickness is not particularly limited but desirably 200 μm to 3000 μm.And, the ratio of respective layers in thickness is not particularlylimited, but it is preferable that the skin layer is 10 to 25% of thewhole, the intermediate layer is 10 to 30% of the whole, the adhesivelayer is 3 to 15% of the whole, the innermost layer is 5 to 20% of thewhole, and the intermediate core layer is 10 to 72% of the whole.

Embodiment 1-6 maintains the same effect as Embodiment 1-5 exceptingtransparency, and a returned item can be used as the resin for theintermediate core layer. Thus, it is superior in the cost performanceand can be applied suitably to usage not requiring transparency.

Embodiment 1-7

Embodiment 1-7 is a laminate having a five-layered structure formed of acore layer and a skin layer which is laminated on either side of thecore layer, wherein the core layer is formed of an innermost layer andan adhesive layer which is laminated on either side of the innermostlayer.

The innermost layer is formed of polyamide (MXD6) which is obtained bymelt polymerization of a diamine component containing 70 mol % or moreof metaxylylene diamine and a dicarboxylic acid component containing 70mol % or more of adipic acid, and the same polyamide (MXD6) as thatforming the core layer of Embodiment 1-5 can be used.

The adhesive layer can be the same adhesive layer as that of Embodiment1-5.

Thickness is not particularly limited but desirably 200 μm to 3000 μm.And, the ratio of respective layers in thickness is not particularlylimited, but it is preferable that the skin layer is 50 to 92% of thewhole, the adhesive layer is 3 to 25% of the whole, and the innermostlayer is 5 to 25% of the whole.

Embodiment 1-7 maintains the same effect as Embodiment 1-1 exceptingheat resistance and excels Embodiments 1-1 and 1-3 in oxygen barrierproperties. Its heat resistance is sufficient to withstand sterilizationconditions of aseptic filling food and, therefore, it can be usedsuitably as a packaging container for aseptic filling food and drink.

Embodiment 1-8

Embodiment 1-8 is a laminate having a six-layered structure which has anintermediate core layer formed between the skin layer and the adhesivelayer on one side of the core layer in the laminated structure ofEmbodiment 1-7.

The intermediate core layer is formed of a amorphous resin whichincludes a thermoplastic polyester resin as the main constituent. Acrystalline resin is not desirable because whitening may occur whenforming.

Here, the same thermoplastic polyester resin as that described inconnection with the core layer of Embodiment 1-1 can be used. Theabove-described main constituent means 50 wt % or more, and desirably 93wt % or more, of the thermoplastic polyester resin.

Specifically, a polymer alloy consisting of 13 wt % to 90 wt % ofpolyethylene terephthalate (PET), 2 wt % to 42 wt % ofpolyethylene-2,6-naphthalate (PEN), 4 wt % to 25 wt % of polyamide(MXD6) and 4 wt % to 20 wt % of an acid-modified polyolefin resin can beused suitably. And, in a range not changing the molar ratio of2,6-naphthalene group and phenylene group (2,6-naphthalenegroup/phenylene group), polyethylene terephthalate (PET) andpolyethylene-2,6-naphthalate (PEN) may be partly or wholly replaced witha copolymer consisting of 2,6-naphthalene dicarboxylic acid or its loweralkyl ester, terephthalic acid or its lower alkyl ester and ethyleneglycol, or a returned item may be used.

Thickness is not particularly limited but desirably 200 μm to 3000 μm.And, the ratio of respective layers in thickness is not particularlylimited, but it is preferable that the skin layer is 10 to 45% of thewhole, the adhesive layer is 3 to 20% of the whole, the innermost layeris 5 to 25% of the whole, and the intermediate core layer is 10 to 82%of the whole.

Embodiment 1-8 maintains the same effect as Embodiment 1-7 exceptingtransparency, can use a returned item as the resin for the intermediatecore layer and excels in the cost performance. And, it can be usedsuitably as a packaging container for aseptic filling food and drink,which is not required to have transparency.

[Second Laminate]

The second laminate is a laminate which has a core layer and a skinlayer on either side of the core layer.

The skin layer is formed of a polyester copolymer which consists of2,6-naphthalene dicarboxylic acid or its lower alkyl ester, terephthalicacid or its lower alkyl ester, 1,4-cyclohexane dimethanol and ethyleneglycol. Specifically, the polyester copolymer is indicated by a generalformula, HO—(COArCOORO)_(n)—H (n is 100 to 1000, preferably 100 to 400.But, Ar indicates 2,6-naphthalene group and phenylene group, and Rindicates ethylene group and 1,4-cyclohexylene group).

Here, as the lower alkyl ester of 2,6-naphthalene dicarboxylic acid andthe lower alkyl ester of terephthalic acid, the same ones as describedin connection with the skin layer of the first laminate can be used.

The above polyester copolymer is desired that a molar ratio of2,6-naphthalene group and phenylene group (2,6-naphthalenegroup/phenylene group) is 50/50 to 98/2, and preferably 60/40 to 95/5, amolar ratio of 1,4-cyclohexylene group and ethylene group(1,4-cyclohexylene group/ethylene group) is 95/5 to 10/90, preferably60/40 to 10/80, and a molar ratio of a cis form and a trans form(cis/trans) of the 1,4-cyclohexylene group is in a range of 0/100 to40/60.

It has a tendency that, when a ratio of 2,6-naphthalene group exceeds 98mol % and a ratio of phenyl group is less than 2 mol %, recyclingefficiency and heat-sealing properties are degraded, and when the ratioof 2,6-naphthalene group is less than 50 mol % and the ratio of phenylgroup exceeds 50 mol %, the heat resistance, resistance to hot water andresistance to whitening are degraded.

And, when the ratio of 1,4-cyclohexylene group exceeds 95 mol % and theethylene group is less than 5 mol %, crystallizability proceeds, andresistance to whitening in hot water tends to become inferior. When theratio of 1,4-cyclohexylene group is less than 10 mol % and the ethylenegroup exceeds 90 mol %, recycling efficiency and heat-sealing propertiesare degraded, and it has a tendency to become not suitable as apackaging container. Similarly, in the 1,4-cyclohexylene group, when theratio of cis form exceeds 40 mol % in the ratio of cis/trans forms,namely when the ratio of trans form is less than 60 mol %, there is atendency that the heat resistance lowers, and it becomes unsuitable as apackaging container.

Specific examples of the second laminate will be described below, but itis to be noted that the second laminate is not limited to them.

Embodiment 2-1

Embodiment 2-1 is a laminate having a three-layered structure consistingof a core layer and a skin layer laminated on either side of the corelayer.

The core layer is formed of a polymer alloy consisting of aheat-resistant resin and a thermoplastic polyester resin, which contains50 to 65 wt % of the heat-resistant resin, and the same polymer alloy asthat forming the core layer of Embodiment 1-1 can be used.

The core layer has an effect of giving impact resistance to the laminatewhen 2,6-naphthalene group of the polyester copolymer used for the skinlayer is 85 mol % or more (phenylene group is 15 mol % or below) and aneffect of giving impact resistance and heat resistance to the laminatewhen 2,6-naphthalene group is less than 85 mol % (phenylene groupexceeds 15 mol %). When the 2,6-naphthalene group of the polyestercopolymer used for the skin layer is 85 mol % or more and high impactresistance is not required, the core layer may be thermoplasticpolyester not containing a heat-resistant resin. This will be describedlater as Embodiment 2-9.

Thickness is not particularly limited but desirably 200 μm to 3000 μm.And, the ratio of respective layers in thickness is not particularlylimited, but it is preferable that the skin layer is 10 to 40% of thewhole, and the core layer is 90 to 60% of the whole.

Embodiment 2-1 is superior in sealing properties with a lid body, can beclosed tightly by an aluminum closure, excels in recycling efficiencywith the PET resin, and has flavor resistance and aroma retentionsufficient not being limited by types of flavors used for jelly, waterice or the like. It is also superior in gas barrier properties (oxygenbarrier properties), impact resistance, cold-impact resistance, heatresistance and transparency and can be used suitably as a packagingcontainer for food and drink, such as jelly containers, water icecontainers and the like.

Embodiment 2-2

Embodiment 2-2 is a laminate having a five-layered structure formed of acore layer, an intermediate layer laminated on either side of the corelayer and a skin layer laminated on the intermediate layer.

The core layer is formed of a amorphous resin which includes athermoplastic polyester resin as the main constituent. A crystallineresin is not desirable because whitening may occur when forming.

Here, the same thermoplastic polyester resin as that described inconnection with the core layer of Embodiment 1-1 can be used. Theabove-described main constituent means 50 wt % or more, and desirably 93wt % or more, of the thermoplastic polyester resin.

Specifically, a polymer alloy of 90 wt % to 45 wt % of polyethyleneterephthalate (PET), 15 wt % to 30 wt % of the polyester copolymer usedfor the skin layer and 15 wt % to 25 wt % of a heat-resistant resin canbe used suitably, and a returned item may be used.

The intermediate layer is formed of a polymer alloy consisting of aheat-resistant resin and a thermoplastic polyester resin, which contains50 to 65 wt % of the heat-resistant resin. The same polymer alloy asthat forming the core layer of Embodiment 1-1 can be used.

The intermediate layer has an effect of giving impact resistance to thelaminate when 2,6-naphthalene group of the polyester copolymer used forthe skin layer is 85 mol % or more (phenylene group is 15 mol % orbelow) and an effect of giving impact resistance and heat resistance tothe laminate when the 2,6-naphthalene group is less than 85 mol %(phenylene group exceeds 15 mol %).

Thickness is not particularly limited but desirably 200 μm to 3000 μm.And, the ratio of respective layers in thickness is not particularlylimited, but it is preferable that the skin layer is 10 to 45% of thewhole, the intermediate layer is 10 to 45% of the whole, the core layeris 80 to 10% of the whole, and it is more desirable that the skin layeris 10 to 30% of the whole, the intermediate layer is 20 to 40% of thewhole, and the core layer is 70 to 30% of the whole.

Embodiment 2-2 maintains the same effect as Embodiment 2-1 and can alsouse as a resin for the core layer a returned item, which is produced atthe time of sheet forming and container forming, and it is superior inthe cost performance.

Embodiment 2-3

Embodiment 2-3 is a laminate having a three-layered structure consistingof a core layer and a skin layer laminated on either side of the corelayer.

The core layer is formed of a copolymer having a glass transition pointof 110° C. or more and consisting of 2,6-naphthalene dicarboxylic acidor its lower alkyl ester, terephthalic acid or its lower alkyl ester andethylene glycol or a polymer alloy having a glass transition point of110° C. or more and consisting of polyethylene terephthalate andpolyethylene-2,6-naphthalate. And, the same copolymer or polymer alloyas that forming the core layer of Embodiment 1-3 can be used.

Thickness is not particularly limited but desirably 200 μm to 3000 μm.And, the ratio of respective layers in thickness is not particularlylimited, but it is preferable that the skin layer is 10 to 40% of thewhole, and the core layer is 90 to 60% of the whole.

Embodiment 2-3 maintains the same effect as Embodiment 2-1 and excelsEmbodiment 2-1 in oxygen barrier properties.

Embodiment 2-4

Embodiment 2-4 is a laminate having a five-layered structure consistingof a core layer, an intermediate layer laminated on either side of thecore layer and a skin layer laminated on the intermediate layer.

The core layer is formed of a amorphous resin which includes athermoplastic polyester resin as the main constituent. A crystallineresin is not desirable because whitening may occur when forming.

Here, the same thermoplastic polyester resin as that described inconnection with the core layer of Embodiment 1-1 can be used. Theabove-described main constituent means 50 wt % or more, and desirably 93wt % or more, of the thermoplastic polyester resin.

Specifically, a polymer alloy consisting of 13 wt % to 90 wt % ofpolyethylene terephthalate (PET), 8 wt % to 42 wt % ofpolyethylene-2,6-naphthalate (PEN) and 2 wt % to 45 wt % of thepolyester copolymer used for the skin layer can be used suitably. And,in a range without changing a molar ratio of 2,6-naphthalene group andphenylene group (2,6-naphthalene group/phenylene group), polyethyleneterephthalate (PET) and polyethylene-2,6-naphthalate (PEN) may be partlyor wholly replaced with a copolymer consisting of 2,6-naphthalenedicarboxylic acid or its lower alkyl ester, terephthalic acid or itslower alkyl ester and ethylene glycol, and a returned item may be used.

The intermediate layer is formed of a copolymer having a glasstransition point of 110 or more and consisting of 2,6-naphthalenedicarboxylic acid or its lower alkyl ester, terephthalic acid or itslower alkyl ester and ethylene glycol or a polymer alloy having a glasstransition point of 110° C. or more and consisting of polyethyleneterephthalate and polyethylene-2,6-naphthalate. And, the same copolymeror polymer alloy as that forming the core layer of Embodiment 1-3 can beused.

Thickness is not particularly limited but desirably 200 μm to 3000 μm.And, the ratio of respective layers in thickness is not particularlylimited, but it is preferable that the skin layer is 10 to 45% of thewhole, the intermediate layer is 10 to 45% of the whole, and the corelayer is 80 to 10% of the whole. And, it is more desirable that the skinlayer is 10 to 30% of the whole, the intermediate layer is 20 to 40% ofthe whole, and the core layer is 70 to 30% of the whole.

Embodiment 2-4 maintains the same effect as Embodiment 2-3 and can alsouse a returned item as a resin for the core layer, and it is superior inthe cost performance.

Embodiment 2-5

Embodiment 2-5 is a laminate having a seven-layered structure consistingof a core layer, an intermediate layer laminated on either side of thecore layer and a skin layer laminated on the intermediate layer, inwhich the core layer consists of an innermost layer and an adhesivelayer laminated on either side of the innermost layer.

The innermost layer is formed of polyamide (MXD6) which is obtained bymelt polymerization of a diamine component containing 70 mol % or moreof metaxylylene diamine and a dicarboxylic acid component of 70 mol % ormore of adipic acid, and the same polyamide (MXD6) as that forming thecore layer of Embodiment 1-5 can be used.

The adhesive layer can be the same adhesive layer as that of Embodiment1-5.

The intermediate layer is formed of a polymer alloy consisting of aheat-resistant resin and a thermoplastic polyester resin, which contains50 to 65 wt % of the heat-resistant resin, and the same polymer alloy asthat forming the core layer of Embodiment 1-1 can be used.

Thickness is not particularly limited but desirably 200 μm to 3000 μm.And, the ratio of respective layers in thickness is not particularlylimited, but it is preferable that the skin layer is 10 to 82% of thewhole, the intermediate layer is 10 to 45% of the whole, the adhesivelayer is 3 to 20% of the whole, and the innermost layer is 5 to 25% ofthe whole.

Embodiment 2-5 maintains the same effect as Embodiment 2-1 and excelsEmbodiments 2-1 and 2-3 in oxygen barrier properties.

Embodiment 2-6

Embodiment 2-6 is a laminate having an eight-layered structure which hasan intermediate core layer formed between the intermediate layer and theadhesive layer on one side of the core layer in the laminated structureof Embodiment 2-5.

The intermediate core layer is formed of a amorphous resin whichincludes a thermoplastic polyester resin as the main constituent. Acrystalline resin is not desirable because whitening may occur whenforming.

Here, the same thermoplastic polyester resin as that described inconnection with the core layer of Embodiment 1-1 can be used. Theabove-described main constituent means 50 wt % or more, and desirably 93wt % or more, of the thermoplastic polyester resin.

Specifically, a polymer alloy consisting of 10 wt % to 82 wt % ofpolyethylene terephthalate (PET), 5 wt % to 30 wt % of a polyestercopolymer used for the skin layer, 5 wt % to 20 wt % of a heat-resistantresin, 4 wt % to 25 wt % of polyamide (MXD6) and 4 wt % to 15 wt % of anacid-modified polyolefin resin can be used suitably, and a returned itemmay be used.

Thickness is not particularly limited but desirably 200 μm to 3000 μm.And, the ratio of respective layers in thickness is not particularlylimited, but it is preferable that the skin layer is 10 to 25% of thewhole, the intermediate layer is 10 to 30% of the whole, the adhesivelayer is 3 to 20% of the whole, the innermost layer is 5 to 20% of thewhole, and the intermediate core layer is 10 to 72% of the whole.

Embodiment 2-6 maintains the same effect as Embodiment 2-5 exceptingtransparency, and a returned item can be used as a resin for theintermediate core layer, excelling in the cost performance. And, it canbe applied suitably to usage not requiring transparency.

Embodiment 2-7

Embodiment 2-7 is a laminate having a five-layered structure consistingof a core layer and a skin layer laminated on either side of the corelayer, in which the core layer consists of an innermost layer and anadhesive layer laminated on either side of the innermost layer.

The innermost layer is formed of polyamide (MXD6) which is obtained bymelt polymerization of a diamine component containing 70 mol % or moreof metaxylylene diamine and a dicarboxylic acid component containing 70mol % or more of adipic acid, and the same polyamide (MXD6) as thatforming the core layer of Embodiment 1-5 can be used.

The adhesive layer can be the same adhesive layer as that of Embodiment1-5.

Thickness is not particularly limited but desirably 200 μm to 3000 μm.And, the ratio of respective layers in thickness is not particularlylimited, but it is preferable that the skin layer is 50 to 92% of thewhole, the adhesive layer is 3 to 25% of the whole, and the innermostlayer is 5 to 25% of the whole.

Embodiment 2-7 maintains the same effect as Embodiment 2-1 exceptingheat resistance and excels Embodiments 2-1 and 2-3 in the oxygen barrierproperties. Its heat resistance is sufficient to withstand sterilizationconditions for aseptic filling food and, therefore, it can be usedsuitably as a packaging container for aseptic filling food and drink.

Embodiment 2-8

Embodiment 2-8 is a laminate having a six-layered structure which has anintermediate core layer formed between the skin layer and adhesive layeron one side of the core layer in the laminated structure of Embodiment2-7.

The intermediate core layer is formed of a amorphous resin whichincludes a thermoplastic polyester resin as the main constituent. Acrystalline resin is not desirable because whitening may occur whenforming.

Here, the same thermoplastic polyester resin as that described inconnection with the core layer of Embodiment 1-1 can be used. Theabove-described main constituent means 50 wt % or more, and desirably 93wt % or more, of the thermoplastic polyester resin.

Specifically, a polymer alloy consisting of 10 wt % to 87 wt % ofpolyethylene terephthalate (PET), 5 wt % to 45 wt % of a polyestercopolymer used for the skin layer, 4 wt % to 25 wt % of polyamide (MXD6)and 4 wt % to 20 wt % of an acid-modified polyolefin resin can be usedsuitably, and a returned item may be used.

Thickness is not particularly limited but desirably 200 μm to 3000 μm.And, the ratio of respective layers in thickness is not particularlylimited, but it is preferable that the skin layer is 10 to 45% of thewhole, the adhesive layer is 3 to 20% of the whole, the innermost layeris 5 to 25% of the whole, and the intermediate core layer is 10 to 82%of the whole.

Embodiment 2-8 maintains the same effect as Embodiment 2-7 exceptingtransparency and a returned item can be used as a resin for theintermediate core layer, excelling in the cost performance. And, it canbe suitably used as a packaging container for aseptic filling food anddrink not requiring transparency.

Embodiment 2-9

Embodiment 2-9 is a laminate having a three-layered structure consistingof a core layer and a skin layer laminated on either side of the corelayer.

The skin layer is formed of a polyester copolymer in which a molar ratioof 2,6-naphthalene group and phenylene group (2,6-naphthalenegroup/phenylene group) is 85/15 to 98/2, preferably 85/15 to 95/5.

The core layer is formed of a amorphous resin which includes athermoplastic polyester resin as the main constituent. A crystallineresin is not desirable because whitening may occur when forming.

Here, the same thermoplastic polyester resin as that described inconnection with the core layer of Embodiment 1-1 can be used. Theabove-described main constituent means 50 wt % or more, and desirably 93wt % or more, of the thermoplastic polyester resin.

Specifically, the polyester copolymer used for the skin layer can beused suitably in view of recycling efficiency, and a returned item maybe used in view of cost efficiency.

Embodiment 2-9 does not need to have a layer formed of a polymer alloy,which consists of a heat-resistant resin and a thermoplastic polyesterresin containing 50 to 65 wt % of the heat-resistant resin, as inEmbodiments 2-1 and 2-2, because the polyester copolymer forming theskin layer is superior in heat resistance. Thus, it excels in costefficiency.

[First Laminate and Second Laminate]

A method of producing a laminate of the present invention is notparticularly limited, and the resins which form the respective layersare formed into a laminate by a co-extrusion process or extrusionlaminating process. Thus, a conventionally known method can be used forproduction.

The laminate of the present invention is a superior material for sheetforming of a cup-shaped packaging container or a tray-shaped packagingcontainer for food and drink having a pH of less than 4.0 such as jelly(also water ice in the case of the second laminate), forhigh-temperature circulating food which is subject to heat sterilizationprocessing, or for aseptic filling food and drink, and this laminate canalso be used to form a packing bag for retort food.

[Packaging Container]

The packaging container of the present invention has a container bodywhich is formed of the above-mentioned laminate and has an opening atthe upper portion. Specifically, it consists of the container body and alid body for opening/closing the opening to allow loading/unloading offood or drink.

For example, as shown in FIG. 1 and FIG. 2, the above-describedlaminated sheet is formed into the container body having an invertedtruncated cone shape by pneumatic molding, preferably by using asimultaneous punching pneumatic molding machine, and it has a flange atthe top end of the body section and a bottom at the lower end.

The lid body has the surface layer formed of a thermoplastic polyesterresin and bonded to the flange of the container body by heating andwelding (heat sealing) or radio frequency induction heating so to shieldthe opening of the container body. The lid body is not particularlylimited as long as the surface layer is formed of a thermoplasticpolyester resin, and an aluminum substrate (aluminum foil), a filmsubstrate or the like can be used, but the first laminate and thelaminate of Embodiment 2-9 are desired to be a film substrate in orderto obtain sufficient airtightness.

EXAMPLES

The present invention will be described in further detail with referenceto Examples.

Evaluation methods in Examples are as follows.

(1) Heat Resistance

{circle over (1)} Shrinkage of Container

The container filled with hot water of 65° C. was sealed with the lidbody, heated at 87° C. for 30 minutes (container shrinkage A:sterilization condition for food having a pH of less than 4.0), orsprayed with a hydrogen peroxide solution heated to 120° C. for twoseconds, dried with hot air of 140° C. for four seconds (containershrinkage B: sterilization condition for aseptic filling food), and therate of change before and after the treatment was measured (the capacitywas measured on a water weight basis). When a capacity change was within2.5%, it was indicated by ◯, and when the capacity change exceeded 2.5%,it was indicated by X.

An empty container was also subjected to the same test, and when thecapacity change was within 2.5%, it was indicated by ◯, and when thecapacity change exceeded 2.5%, it was indicated by X.

{circle over (2)} Change in Shape

After the filled container was measured for its container shrinkage, thesample was visually observed for buckling (the bottom swelled to cause achange in shape) and shrinkage of the body section. No change wasindicated by ◯, and buckling or shrinkage of the body section wasindicated by X.

(2) Impact Resistance

{circle over (1)} Drop Test

The container filled with hot water of 65° C. was sealed with the lidbody and thermally treated at 87° C. for 30 minutes (drop test A:sterilization condition for food having a pH of less than 4.0). Thecontainer filled its 80% with hot water of 65° C. was sealed with thelid body (drop test B: condition for aseptic filling food) and leftstanding at 4° C. for 24 hours. Such a container was dropped two timescontinuously from a height of 80 cm for bottom face vertical dropping(condition for the container having a content of less than 100 g. Theabove severe condition was adopted because, when the content was 100 gor more and less than 400 g, the test condition was a drop from a heightof 50 cm.) and dropped two times continuously from a height of 50 cm forside face vertical dropping. And, evaluation was made according to thefollowing criteria.

-   ◯: No leakage.-   Δ: Leaked when dropped two times.-   X: Leaked when dropped one time.    {circle over (2)} Grip Test

The container was left standing at 4° C., hardly squeezed in verticaland horizontal directions, and visually observed for a level ofbreakage. When the flange was free from a crack, it was indicated by ◯,when a crack was caused by squeezing in either of the directions, it wasindicated by Δ, and when cracks were caused by squeezing in bothdirections, it was indicated by X.

(3) Gas Barrier Properties (Oxygen Permeability)

Oxygen permeability of each container was measured by “OX-TRAN 2/20”manufactured by MOCON under conditions of 23%, a relative humidity of60% and 24 hours.

(4) Sealing Properties

After the container body and the lid body were heat-sealed (heat sealconditions: single flat sealing at 180° C. for 1.5 seconds for a filmclosure, and single flat sealing at 210° C. for 1.5 seconds for analuminum closure), and the heat-sealed portion was cut to a width of 15mm. Its peel strength was measured by a strograph manufactured by SugaTest Instruments at a peel angle of 90° and a rate of pulling of 100mm/min. Evaluation was made according to the following criteria.

-   ⊚: 1.5 kg/15 mm or more-   ◯: 0.8 kg to less than 1.5 kg/15 mm-   X: Less than 0.8 kg/15 mm.    (5) Transparency

Haze of the sheet was measured by HR-100 of MURAKAMI COLOR RESEARCHLABORATORY according to JIS K7105.

(6) Ultraviolet Barrier Properties

Light transmittance of the sheet was measured by a Hitachispectrophotometer U-4000, and evaluation was made according to thefollowing criteria.

-   ◯: In the range of 260 nm to 370 nm, 10% or below-   Δ: In the range of 260 nm to 340 nm, 10% or below    -   In the range of 340 nm to 370 nm, 10% to 80%-   X: In the range of 260 nm to 300 nm, 15% to 70%    -   In the range of 300 nm to 370 nm, 70% or more.        (7) Flavor Resistance

Various kinds of flavors (extracts from natural juice) of NARIZUKACorporation, Ltd. shown in Tables 1 to 9 each were put in the containerbody by 0.28% of the capacity of the container body, water of 40° C. orbelow was charged in it, and the container was sealed with the lid bodyand thermally treated at 87° C. for 30 minutes (flavor resistance A:sterilization condition for food with a pH of less than 4.0), or anaqueous solution having various kinds of flavors shown in Tables 1 to 9each added by 0.28% of the capacity of the container body was heated to65° C. and charged into the container, the container was sealed with thelid body (flavor resistance B: condition for aseptic filling food), andthe state of the container body was visually observed. Six samples ofthe respective flavors were evaluated. No change was indicated by ◯, aslight change was indicated by Δ, and whitening was indicated by X.

The resins used in Examples are as follows.

-   Polyethylene terephthalate (PET): Brand name “NEH-2070” manufactured    by Unitika Ltd.-   Polyarylate resin (PAR): Brand name “U-100” manufactured by Unitika    Ltd. (Tg=193° C. and an Izod impact test value of 218.5 J/m when    tested with a ⅛″ notch under conditions of 23° C. and a relative    humidity of 50).-   Polyethylene-2,6-naphthalate (PEN): Brand name “TN-8060”    manufactured by Teijin Chemicals Ltd.-   PET-PAR based polymer alloy: Brand name “U-8000” manufactured by    Unitika Ltd. (PAR (Tg=193° C. and an Izod impact test value of 218.5    J/m when tested with a ⅛′ notch under 23° C. and a relative humidity    of 50%) 60 wt %, PET 40 wt %).-   Polyamide (MXNy): Brand name “MX Nylon S6011” (same as MXD6)    manufactured by Mitsubishi Gas Chemical Co., Inc.-   Adhesive agent (AD): Brand name “MODIC F534” manufactured by    Mitsubishi Chemical Corporation.

Example 1 Embodiment 1-2

Using the resins shown below, an 800 μm thick laminated sheet having afive-layered structure (a ratio of layer thickness: skin layer10%/intermediate layer 10%/core layer 60%/intermediate layer 10%/skinlayer 10%) was produced by a co-extrusion process.

-   Core layer: Polymer alloy of PET, PEN and PAR (PET 80 wt %, PEN 10    wt %, PAR 10 wt %).-   Intermediate layer: PET-PAR based polymer alloy.-   Skin layer: Polymer alloy of PET and PEN (Tg=100° C., a molar ratio    of 2,6-naphthalene group and phenylene group (2,6-naphthalene    group/phenylene group) is 60/40).

This laminated sheet was formed into the cup-shaped container bodyhaving an inside capacity of 110 cc and a height of 47.3 mm as shown inFIG. 1 by a simultaneous punching pneumatic molding machine andevaluated. The results are shown in Table 1.

For the lid body, an easy-peel transparent film having the layerstructure indicated below was used.

-   Nylon (NY) 15 μm/barrier nylon (NY) 15 μm/special polyethylene (PE)    30 μm/polyester coat 2 μm.

Example 2 Embodiment 1-1

Using the resins shown below, an 800 μm thick laminated sheet having athree-layered structure (a ratio of layer thickness: skin layer 10%/corelayer 80%/skin layer 10%) was produced by a co-extrusion process. Thislaminated sheet was formed into a container body having the same sizeand shape as that of Example 1 and evaluated. The results are shown inTable 1.

-   Core layer: PET-PAR based polymer alloy.

Skin layer: Polymer alloy of PET and PEN used as the resin for the skinlayer in Example 1. TABLE 1 Example 1 Example 2 Heat Container ◯/◯ ◯/◯resistance (shrinkage A Filled container/empty container) Change inshape ◯ ◯ Impact Drop test A resistance (Bottom face ◯/◯ ◯/◯ drop/sideface drop) Grip test ◯ ◯ Gas barrier properties 0.08 0.10 (cc/container· 24 hr · atm) Sealing properties ◯ ◯ Transparency (%) 0.69 0.93Ultraviolet barrier ◯ ◯ properties Flavor Muscat FLA ◯/◯/◯/◯/◯/◯◯/◯/◯/◯/◯/◯ resistance A 0076-U Muscat FLA 1686 ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯Peach FLA 0048-V ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ Peach FLA 1186 ◯/◯/◯/◯/◯/◯◯/◯/◯/◯/◯/◯ Orange ESS ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ Valencia Orange◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ ESS Super 1656 Apple FLA 0158-U ◯/◯/◯/◯/◯/◯◯/◯/◯/◯/◯/◯ Apple FLA 0173-U ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ Lemon ESS◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ La-france FLA ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ 0061-VPlum FLA 0027- ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ RNEW Plum ESS 2226 ◯/◯/◯/◯/◯/◯◯/◯/◯/◯/◯/◯ Pear FLA 1700 ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯

Example 3 Embodiment 1-4

Using the resins shown below, an 800 μm thick laminated sheet having afive-layered structure (a ratio of layer thickness: skin layer10%/intermediate layer 10%/core layer 60%/intermediate layer 10%/skinlayer 10%) was produced by a co-extrusion process. This laminated sheetwas formed into a container body having the same size and shape as thatof Example 1 and evaluated. The results are shown in Table 2.

-   Core layer: Polymer alloy of PET, copolymer used as the resin for    the intermediate layer and PEN (molar ratio of 2,6-naphthalene group    and phenylene group (2,6-naphthalene group/phenylene group) is    16/84).-   Intermediate layer: Copolymer of 2,6-naphthalene dicarboxylic acid,    terephthalic acid and ethylene glycol (Tg=115° C., molar ratio of    2,6-naphthalene group and phenylene group (2,6-naphthalene    group/phenylene group) is 92/8).-   Skin layer: Polymer alloy of PET and PEN used as the resins for the    skin layer in Example 1.

Example 4 Embodiment 1-3

Using the resins shown below, an 800 μm thick laminated sheet having athree-layered structure (a ratio of layer thickness: skin layer 10%/corelayer 80%/skin layer 10%) was produced by a co-extrusion process. Thislaminated sheet was formed into a container body having the same sizeand shape as that of Example 1 and evaluated. The results are shown inTable 2.

-   Core layer: Copolymer used as the resin for the intermediate layer    in Example 3.

Skin layer: Polymer alloy of PET and PEN used as the resins for the skinlayer in Example 1. TABLE 2 Example 3 Example 4 Heat Container ◯/◯ ◯/◯resistance shrinkage A (Filled container/empty container) Change inshape ◯ ◯ Impact Drop test A ◯/Δ Δ/Δ resistance (Bottom face drop/sideface drop) Grip test ◯ Δ Gas barrier properties 0.04 0.03 (cc/container· 24 hr · atm) Sealing properties ◯ ◯ Transparency (%) 0.98 0.56Ultraviolet barrier ◯ ◯ properties Flavour Muscat FLA ◯/◯/◯/◯/◯/◯◯/◯/◯/◯/◯/◯ resistance A 0076-U Muscat FLA 1686 ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯Peach FLA 0048-V ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ Peach FLA 1186 ◯/◯/◯/◯/◯/◯◯/◯/◯/◯/◯/◯ Orange ESS ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ Valencia Orange◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ ESS Super 1656 AppleFLA 0158-U ◯/◯/◯/◯/◯/◯◯/◯/◯/◯/◯/◯ Apple FLA 0173-U ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ Lemon ESS◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ La-france FLA ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ 0061-VPlum FLA 0027- ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ RNEW Plum ESS 2226 ◯/◯/◯/◯/◯/◯◯/◯/◯/◯/◯/◯ Pear FLA 1700 ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯

Example 5 Embodiment 1-5

Using the resins shown below, an 800 μm thick laminated sheet having aseven-layered structure (a ratio of layer thickness: skin layer30%/intermediate layer 10%/adhesive layer 2.5%/innermost layer15%/adhesive layer 2.5%/intermediate layer 10%/skin layer 30%) wasproduced by a co-extrusion process. This laminated sheet was formed intoa container body having the same size and shape as that of Example 1 andevaluated. The results are shown in Table 3.

-   Innermost layer: MXNy-   Adhesive layer: AD-   Intermediate layer: PET-PAR based polymer alloy-   Skin layer: Polymer alloy of PET and PEN used as the resins for the    skin layer in Example 1.

Example 6 Embodiment 1-6

Using the resins shown below, an 800 μm thick laminated sheet having aneight-layered structure (a ratio of layer thickness: skin layer10%/intermediate layer 10%/intermediate core layer 40%/adhesive layer2.5%/innermost layer 15%/adhesive layer 2.5%/intermediate layer 10%/skinlayer 10%) was produced by a co-extrusion process. This laminated sheetwas formed into a container body having the same size and shape as thatof Example 1 and evaluated. The results are shown in Table 3.

-   Innermost layer: MXNy-   Adhesive layer: AD-   Intermediate core layer: Polymer alloy of PET, PEN, PAR, AD and MXNy    (PET 76 wt %, PEN 6 wt %, PAR 6 wt %, AD 5 wt %, MXNy 7 wt %).-   Intermediate layer: PET-PAR based polymer alloy.

Skin layer: Polymer alloy of PET and PEN used as the resins for the skinlayer in Example 1. TABLE 3 Example 5 Example 6 Heat Container ◯/◯ ◯/◯resistance shrinkage A (Filled container/empty container) Change inshape ◯ ◯ Impact Drop test A ◯/◯ ◯/◯ resistance (Bottom face drop/sideface drop) Grip test ◯ ◯ Gas barrier properties 0.01  0.01 (cc/container· 24 hr · atm) Sealing properties ◯ ◯ Transparency (%) 1.0 80Ultraviolet barrier ◯ ◯ properties Flavour Muscat FLA ◯/◯/◯/◯/◯/◯◯/◯/◯/◯/◯/◯ resistance A 0076-U Muscat FLA 1686 ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯Peach FLA 0048-V ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ Peach FLA 1186 ◯/◯/◯/◯/◯/◯◯/◯/◯/◯/◯/◯ Orange ESS ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ Valencia Orange◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ ESS Super 1656 Apple FLA 0158-U ◯/◯/◯/◯/◯/◯◯/◯/◯/◯/◯/◯ Apple FLA 0173-U ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ Lemon ESS◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ La-france FLA ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ 0061-VPlum FLA 0027- ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ RNEW Plum ESS 2226 ◯/◯/◯/◯/◯/◯◯/◯/◯/◯/◯/◯ Pear FLA 1700 ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯

Example 7 Embodiment 1-7

Using the resins shown below, an 800 μm thick laminated sheet having afive-layered structure (a ratio of layer thickness: skin layer40%/adhesive layer 5%/innermost layer 12%/adhesive layer 5%/skin layer38%) was produced by a co-extrusion process. This laminated sheet wasformed into a container body having the same size and shape as that ofExample 1 and evaluated. The results are shown in Table 4.

-   Innermost layer: MXNy-   Adhesive layer: AD-   Skin layer: Polymer alloy of PET and PEN used as the resins for the    skin layer in Example 1.

Example 8 Embodiment 1-8

Using the resins shown below, an 800 μm thick laminated sheet having asix-layered structure (a ratio of layer thickness: skin layer10%/intermediate core layer 60%/adhesive layer 5%/innermost layer10%/adhesive layer 5%/skin layer 10%) was produced by a co-extrusionprocess. This laminated sheet was formed into a container body havingthe same size and shape as that of Example 1 and evaluated. The resultsare shown in Table 4.

-   Innermost layer: MXNy-   Adhesive layer: AD-   Intermediate core layer: Polymer alloy of PET, PEN, AD and MXNy (PET    82 wt %, PEN 8 wt %, AD 5 wt %, MXNy 5 wt %).

Skin layer: Polymer alloy of PET and PEN used as the resins for the skinlayer in Example 1. TABLE 4 Example 7 Example 8 Heat Container ◯/◯ ◯/◯resistance shrinkage B (Filled container/empty container) Change inshape ◯ ◯ Impact Drop test B ◯/◯ ◯/◯ resistance (Bottom face drop/sideface drop) Grip test ◯ ◯ Gas barrier properties 0.01  0.01 (cc/container· 24 hr · atm) Sealing properties ◯ ◯ Transparency (%) 0.90 80Ultraviolet barrier ◯ ◯ properties Flavour Muscat FLA ◯/◯/◯/◯/◯/◯◯/◯/◯/◯/◯/◯ resistance B 0076-U Muscat FLA 1686 ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯Peach FLA 0048-V ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ Peach FLA 1186 ◯/◯/◯/◯/◯/◯◯/◯/◯/◯/◯/◯ Orange ESS ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ Valencia Orange◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ ESS Super 1656 Apple FLA 0158-U ◯/◯/◯/◯/◯/◯◯/◯/◯/◯/◯/◯ Apple FLA 0173-U ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ Lemon ESS◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ La-france FLA ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ 0061-VPlum FLA 0027- ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ RNEW Plum ESS 2226 ◯/◯/◯/◯/◯/◯◯/◯/◯/◯/◯/◯ Pear FLA 1700 ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯

Example 9 Embodiment 2-2

Using the resins shown below, an 800 μm thick laminated sheet having afive-layered structure (a ratio of layer thickness: skin layer10%/intermediate layer 10%/core layer 60%/intermediate layer 10%/skinlayer 10%) was produced by a co-extrusion process. This laminated sheetwas formed into a container body having the same size and shape as thatof Example 1 and evaluated. The results are shown in Table 5.

-   Core layer: Polymer alloy of PET, a polyester copolymer used as the    resin for the skin layer and PAR (PET 80 wt %, polyester copolymer    10 wt %, PAR 10 wt %).-   Intermediate layer: PET-PAR based polymer alloy.-   Skin layer: Polyester copolymer of 2,6-naphthalene dicarboxylic    acid, terephthalic acid, 1,4-cyclohexane dimethanol and ethylene    glycol [a molar ratio of 2,6-naphthalene group and phenylene group    (2,6-naphthalene group/phenylene group) is 60/40, a molar ratio of    1,4-cyclohexylene group and ethylene group (1,4-cyclohexylene    group/ethylene group) is 40/60, a molar ratio of the cis form and    the trans form (cis/trans) of 1,4-cyclohexylene group is 30/70].

For the lid body, an aluminum lid material having the layer structurebelow and manufactured by Showa Denko Packaging Co., Ltd. was used.

-   Polyethylene terephthalate (PET) 25 μm/aluminum (AL) 30 μm/polyester    sealant 3 to 5 μm.

Example 10 Embodiment 2-1

Using the resins shown below, an 800 μm thick laminated sheet having athree-layered structure (a ratio of layer thickness: skin layer 10%/corelayer 80%/skin layer 10%) was produced by a co-extrusion process. Thislaminated sheet was formed into a container body having the same sizeand shape as that of Example 1 and evaluated in the same way as inExample 9. The results are shown in Table 5.

-   Core layer: PET-PAR based polymer alloy

Skin layer: Polyester copolymer used as the resin for the skin layer inExample 9. TABLE 5 Example 9 Example 10 Heat Container ◯/◯ ◯/◯resistance shrinkage A (Filled container/empty container) Change inshape ◯ ◯ Impact Drop test A ◯/◯ ◯/◯ resistance (Bottom face drop/sideface drop) Grip test ◯ ◯ Gas barrier properties 0.08 0.13 (cc/container· 24 hr · atm) Sealing properties ⊚ ⊚ Transparency (%) 0.61 0.52Ultraviolet barrier ◯ ◯ properties Flavour Muscat FLA ◯/◯/◯/◯/◯/◯◯/◯/◯/◯/◯/◯ resistance A 0076-U Muscat FLA 1686 ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯Peach FLA 0048-V ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ Peach FLA 1186 ◯/◯/◯/◯/◯/◯◯/◯/◯/◯/◯/◯ Orange ESS ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ Valencia Orange◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ ESS Super 1656 Lemon ESS ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯La-france FLA ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ 0061-V Plum FLA 0027- ◯/◯/◯/◯/◯/◯◯/◯/◯/◯/◯/◯ RNEW Pear FLA 1700 ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯

Example 11 Embodiment 2-4

Using the resins shown below, an 800 μm thick laminated sheet having afive-layered structure (a ratio of layer thickness: skin layer10%/intermediate layer 10%/core layer 60%/intermediate layer 10%/skinlayer 10%) was produced by a co-extrusion process. This laminated sheetwas formed into a container body having the same size and shape as thatof Example 1 and evaluated in the same way as in Example 9. The resultsare shown in Table 6.

-   Core layer: Polymer alloy (PET 81 wt %, copolymer 9 wt %, and    polyester copolymer 10 wt %) of PET, a copolymer used as the resin    for the intermediate layer and a polyester copolymer used as the    resin for the skin layer.-   Intermediate layer: Copolymer used as the resin for the intermediate    layer in Example 3.-   Skin layer: Polyester copolymer used as the resin for the skin layer    in Example 9.

Example 12 Embodiment 2-3

Using the resins shown below, an 800 μm thick laminated sheet having athree-layered structure (a ratio of layer thickness: skin layer 10%/corelayer 80%/skin layer 10%) was produced by a co-extrusion process. Thislaminated sheet was formed into a container body having the same sizeand shape as that of Example 1 and evaluated by the same way as inExample 9. The results are shown in Table 6.

-   Core layer: Copolymer used as the resin for the intermediate layer    in Example 3.

Skin layer: Polyester copolymer used as the resin for the skin layer inExample 9. TABLE 6 Example 11 Example 12 Heat Container ◯/◯ ◯/◯resistance shrinkage A (Filled container/empty container) Change inshape ◯ ◯ Impact Drop test A ◯/◯ ◯/Δ resistance (Bottom face drop/sideface drop) Grip test ◯ ◯ Gas barrier properties 0.04 0.03 (cc/container· 24 hr · atm) Sealing properties ⊚ ⊚ Transparency (%) 0.65 0.40Ultraviolet barrier ◯ ◯ properties Flavor Muscat FLA ◯/◯/◯/◯/◯/◯◯/◯/◯/◯/◯/◯ resistance A 0076-U Muscat FLA 1686 ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯Peach FLA 0048-V ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ Peach FLA 1186 ◯/◯/◯/◯/◯/◯◯/◯/◯/◯/◯/◯ Orange ESS ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ Valencia Orange◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ ESS Super 1656 Lemon ESS ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯La-france FLA ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ 0061-V Plum FLA 0027- ◯/◯/◯/◯/◯/◯◯/◯/◯/◯/◯/◯ RNEW Pear FLA 1700 ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯

Example 13 Embodiment 2-5

Using the resins shown below, an 800 μm thick laminated sheet having aseven-layered structure (a ratio of layer thickness: skin layer30%/intermediate layer 10%/adhesive layer 5%/innermost layer15%/adhesive layer 5%/intermediate layer 10%/skin layer 25%) wasproduced by a co-extrusion process. This laminated sheet was formed intoa container body having the same size and shape as that of Example 1 andevaluated in the same way as in Example 9. The results are shown inTable 7.

-   Innermost layer: MXNy-   Adhesive layer: AD-   Intermediate layer: PET-PAR based polymer alloy.-   Skin layer: Polyester copolymer used as the resin for the skin layer    in Example 9.

Example 14 Embodiment 2-6

Using the resins shown below, an 800 μm thick laminated sheet having aneight-layered structure (a ratio of layer thickness: skin layer10%/intermediate layer 10%/intermediate core layer 40%/adhesive layer2.5%/innermost layer 15%/adhesive layer 2.5%/intermediate layer 10%/skinlayer 10%) was produced by a co-extrusion process. This laminated sheetwas formed into a container body having the same size and shape as thatof Example 1 and evaluated in the same way as in Example 9. The resultsare shown in Table 7.

-   Innermost layer: MXNy-   Adhesive layer: AD-   Intermediate core layer: Polymer alloy of PET, polyester copolymer    used as the resin for the skin layer, PAR, AD and MXNy (PET 72 wt %,    a polyester copolymer 10 wt %, PAR 6 wt %, AD 5 wt %, and MXNy 7 wt    %).-   Intermediate layer: PET-PAR based polymer alloy.

Skin layer: Polyester copolymer used as the resin for the skin layer inExample 9. TABLE 7 Example 13 Example 14 Heat Container ◯/◯ ◯/◯resistance shrinkage A (Filled container/empty container) Change inshape ◯ ◯ Impact Drop test A ◯/◯ ◯/◯ resistance (Bottom face drop/sideface drop) Grip test ◯ ◯ Gas barrier properties 0.01  0.01 (cc/container · 24 hr · atm) Sealing properties ⊚ ⊚ Transparency (%) 0.95 84Ultraviolet barrier ◯ ◯ properties Flavor Muscat FLA ◯/◯/◯/◯/◯/◯◯/◯/◯/◯/◯/◯ resistance A 0076-U Muscat FLA 1686 ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯Peach FLA 0048-V ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ Peach FLA 1186 ◯/◯/◯/◯/◯/◯◯/◯/◯/◯/◯/◯ Orange ESS ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ Valencia Orange◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ ESS Super 1656 Lemon ESS ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯La-france FLA ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ 0061-V Plum FLA 0027- ◯/◯/◯/◯/◯/◯◯/◯/◯/◯/◯/◯ RNEW Pear FLA 1700 ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯

Example 15 Embodiment 2-7

Using the resins shown below, an 800 μm thick laminated sheet having afive-layered structure (a ratio of layer thickness: skin layer40%/adhesive layer 5%/innermost layer 15%/adhesive layer 5%/skin layer35%) was produced by a co-extrusion process. This laminated sheet wasformed into a container body having the same size and shape as that ofExample 1 and evaluated in the same way as in Example 9. The results areshown in Table 8.

-   Innermost layer: MXNy-   Adhesive layer: AD-   Skin layer: Polyester copolymer used as the resin for the skin layer    in Example 9.

Example 16 Embodiment 2-8

Using the resins shown below, an 800 μm thick laminated sheet having asix-layered structure (a ratio of layer thickness: skin layer10%/intermediate core layer 60%/adhesive layer 5%/innermost layer10%/adhesive layer 5%/skin layer 10%) was produced by a co-extrusionprocess. This laminated sheet was formed into a container body havingthe same size and shape as that of Example 1 and evaluated in the sameway as in Example 9. The results are shown in Table 8.

-   Innermost layer: MXNy-   Adhesive layer: AD-   Intermediate core layer: Polymer alloy of PET, polyester copolymer    used as the resin for the skin layer, AD and MXNy (PET 80 wt %,    polyester copolymer 10 wt %, AD 5 wt %, and MXNy 5 wt %).

Skin layer: Polyester copolymer used as the resin for the skin layer inExample 9. TABLE 8 Example 15 Example 16 Heat Container ◯/◯ ◯/◯resistance shrinkage B (Filled container/empty container) Change inshape ◯ ◯ Impact Drop test B ◯/◯ ◯/◯ resistance (Bottom face drop/sideface drop) Grip test ◯ ◯ Gas barrier properties 0.01  0.01 (cc/container· 24 hr · atm) Sealing properties ⊚ ⊚ Transparency (%) 0.88 82Ultraviolet barrier ◯ ◯ properties Flavor Muscat FLA ◯/◯/◯/◯/◯/◯◯/◯/◯/◯/◯/◯ resistance B 0076-U Muscat FLA 1686 ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯Peach FLA 0048-V ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ Peach FLA 1186 ◯/◯/◯/◯/◯/◯◯/◯/◯/◯/◯/◯ Orange ESS ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ Valencia Orange◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ ESS Super 1656 Lemon ESS ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯La-france FLA ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ 0061-V Plum FLA 0027- ◯/◯/◯/◯/◯/◯◯/◯/◯/◯/◯/◯ RNEW Pear FLA 1700 ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯

Example 17 Embodiment 2-9

Using the resins shown below, an 800 μm thick laminated sheet having athree-layered structure (a ratio of layer thickness: skin layer 10%/corelayer 80%/skin layer 10%) was produced by a co-extrusion process. Thislaminated sheet was formed into a container body having the same sizeand shape as that of Example 1 and evaluated in the same way as inExample 9. The results are shown in Table 9.

-   Core layer: Returned item of the laminate of this Example (the same    composition as the polyester copolymer used as the resin for the    skin layer).-   Skin layer: Polyester copolymer of 2,6-naphthalene dicarboxylic    acid, terephthalic acid, 1,4-cyclohexane dimethanol and ethylene    glycol [a molar ratio of 2,6-naphthalene group and phenylene group    (2,6-naphthalene group/phenylene group) is 85/15, a molar ratio of    1,4-cyclohexylene group and ethylene group (1,4-cyclohexylene    group/ethylene group) is 40/60, a molar ratio of the cis form and    the trans form (cis/trans) of 1,4-cyclohexylene group is 30/70].

Comparative Example 1

Using the resins shown below, an 800 μm thick laminated sheet having athree-layered structure (a ratio of layer thickness: skin layer 10%/corelayer 80%/skin layer 10%) was produced by a co-extrusion process. Thislaminated sheet was formed into a container body having the same sizeand shape as that of Example 1 and evaluated. The results are shown inTable 9.

-   Core layer: Polymer alloy (PAR 21 wt %, PET 79 wt %) of PET and PAR.

Skin layer: PET-PAR based polymer alloy. TABLE 9 Comparative Example 17Example 1 Heat Container ◯/◯ ◯/◯ resistance shrinkage A (Filledcontainer/empty container) Change in shape ◯ ◯ Impact Drop test A ◯/◯◯/◯ resistance (Bottom face drop/side face drop) Grip test ◯ ◯ Gasbarrier properties 0.06 0.15 (cc/container · 24 hr · atm) Sealingproperties ◯ ◯ Transparency (%) 0.76 0.65 Ultraviolet barrier ◯ Δproperties Flavor Muscat FLA ◯/◯/◯/◯/◯/◯ X/X/X/X/X/X resistance A 0076-UMuscat FLA 1686 ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ Peach FLA 0048-V ◯/◯/◯/◯/◯/◯◯/◯/◯/◯/◯/◯ Peach FLA 1186 ◯/◯/◯/◯/◯/◯ ◯/Δ/Δ/Δ/Δ/Δ Orange ESS◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ Valencia orange ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ ESSSuper 1656 Lemon ESS ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯ La-france FLA ◯/◯/◯/◯/◯/◯◯/◯/◯/◯/◯/◯ 0061-V Plum FLA 0027- ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/Δ RNEW Pear FLA1700 ◯/◯/◯/◯/◯/◯ ◯/◯/◯/◯/◯/◯

INDUSTRIAL APPLICABILITY

As described above, a first laminate of the present invention can beused suitably as a packaging container for food and drink such as ajelly container, which has sufficient flavor resistance and aromaretention not limited by kinds of flavors used for jelly and the like,excels in sealing properties with a lid body, can be sealed with aneasy-peel transparent lid body and also excels in gas barrierproperties, impact resistance, heat resistance, cost efficiency andtransparency.

A second laminate of the present invention can be used suitably as apackaging container for food and drink such as a jelly container, awater ice container or the like, which excels in sealing properties witha lid body, can be sealed with an aluminum closure, excels in recyclingefficiency with a PET resin, has sufficient flavor resistance and aromaretention not limited by kinds of flavors used for jelly, water ice andthe like, and also excels in gas barrier properties, impact resistance,cold-impact resistance, heat resistance, cost efficiency andtransparency.

And, a laminate containing polyamide (MXD6) in the layer structure canbe used suitably as containers for aseptic filling food and drink suchas coffee, juice, and the like.

1. A laminate having a core layer and a skin layer on either side of thecore layer, wherein the skin layer is formed of a copolymer having aglass transition point of 85° C. or more and 115° C. or below andconsisting of 2,6-naphthalene dicarboxylic acid or its lower alkylether, terephthalic acid or its lower alkyl ester and ethylene glycol ora polymer alloy having a glass transition point of 85° C. or more and115° C. or below and consisting of polyethylene terephthalate andpolyethylene-2,6-naphthalate.
 2. The laminate according to claim 1,wherein the core layer is formed of a polymer alloy consisting of athermoplastic polyester resin and a heat-resistant resin, which contains50 to 65 wt % of the heat-resistant resin having an Izod impact testvalue of 80 J/m to 850 J/m when tested with a ⅛″ notch under conditionsof 23° C. and a relative humidity of 50% and having a glass transitionpoint of 140° C. to 250° C.
 3. The laminate according to claim 1,wherein: an intermediate layer is disposed between the core layer andskin layer, the core layer is formed of a amorphous resin including athermoplastic resin as the main constituent, and the intermediate layeris formed of a polymer alloy consisting of a thermoplastic polyesterresin and a heat-resistant resin, which contains 50 to 65 wt % of theheat-resistant resin having an Izod impact test value of 80 J/m to 850J/m when tested with a ⅛″ notch under conditions of 23° C. and arelative humidity of 50% and having a glass transition point of 140° C.to 250° C.
 4. The laminate according to claim 1, wherein the core layeris formed of a copolymer having a glass transition point of 110° C. ormore and consisting of 2,6-naphthlalene dicarboxylic acid or its loweralkyl ester, terephthalic acid or its lower alykyl ester and ethyleneglycol or a polymer alloy having a glass transition point of 110° C. ormore and consisting of polyethylene terephthalate andpolyethylene-2,6-naphthalate.
 5. The laminate according to claim 1,wherein: an intermediate layer is disposed between the core layer andthe skin layer, the core layer is formed of a amorphous resin includinga thermoplastic polyester resin as the main constituent, and theintermediate layer is formed of a copolymer having a glass transitionpoint of 110° C. or more and consisting of 2,6-naphthalene dicarboxylicacid or its lower alkyl ester, terephthalic acid or its lower alkylester and ethylene glycol or a polymer alloy having a glass transitionpoint of 110° C. or more and consisting of polyethylene terephthalateand polyethylene-2,6-naphthalate.
 6. The laminate according to claim 1,wherein: an intermediate layer is disposed between the core layer andthe skin layer, the core layer consists of an innermost layer formed ofpolyamide which is obtained by melt polymerization of a diaminecomponent containing 70 mol % or more of metaxylylene diamine and adicarboxylic acid component containing 70 mol % or more of adipic acidand an adhesive layer laminated on ether side of the innermost layer,and the intermediate layer is formed of a polymer alloy consisting of athermoplastic polyester resin and a heat-resistant resin, which contains50 to 65 wt % of the heat-resistant resin having an Izod impact testvalue of 80 J/m to 850 J/m when tested with a ⅛″ notch under conditionsof 23° C. and a relative humidity of 50% and having a glass transitionpoint of 140° C. to 250° C.
 7. The laminate according to claim 6,wherein an intermediate core layer of a amorphous resin which includes athermoplastic polyester resin as the main constituent is disposedbetween the intermediate layer and the adhesive layer on one side of thecore layer.
 8. The laminate according to claim 1, wherein the core layerconsists of an innermost layer formed of polyamide which is obtained bymelt polymerization of a diamine component containing 70 mol % or moreof metaxylylene diamine and a dicarboxylic acid component containing 70mol % or more of adipic acid and an adhesive layer laminated on etherside of the innermost layer.
 9. The laminate according to claim 8,wherein an intermediate core layer formed of a amorphous resin whichincludes a thermoplastic polyester resin as the main constituent isdisposed between the skin layer and the adhesive layer on one side ofthe core layer.
 10. The laminate according to claim 1, wherein a molarratio of 2,6-naphthalene group and phenylene group (2,6-naphthalenegroup/phenylene group) of the resin forming the skin layer is 30/70 to92/8.
 11. A laminate having a core layer and a skin layer on either sideof the core layer, wherein the skin layer is formed of a polyestercopolymer which consists of 2,6-naphthalene dicarboxylic acid or itslower alkyl ester, terephthalic acid or its lower alkyl ester,1,4-cyclohexane dimethanol and ethylene glycol.
 12. (canceled) 13.(canceled)
 14. (canceled)
 15. (canceled)
 16. (canceled)
 17. (canceled)18. (canceled)
 19. (canceled)
 20. (canceled)
 21. (canceled) 22.(canceled)
 23. The laminate according to claim 2, wherein the polymeralloy of the heat-resistant resin and the thermoplastic polymer resin isa polymer alloy of a polyarylate resin and polyethylene terephthalate.24. The laminate according to claim 1, wherein the resins forming therespective layers are laminated by a co-extrusion process or anextrusion laminating process.
 25. A packaging container having acontainer body with an opening at the upper part, wherein the containerbody is formed of the laminate according to claim
 1. 26. (canceled) 27.The laminate according to claim 2, wherein a molar ratio of2,6-naphthalene group and phenylene group (2,6-naphthalenegroup/phenylene group) of the resin forming the skin layer is 30/70 to92/8.
 28. The laminate according to claim 3, wherein a molar ratio of2,6-naphthalene group and phenylene group (2,6-naphthalenegroup/phenylene group) of the resin forming the skin layer is 30/70 to92/8.
 29. The laminate according to claim 4, wherein a molar ratio of2,6-naphthalene group and phenylene group (2,6-naphthalenegroup/phenylene group) of the resin forming the skin layer is 30/70 to92/8.
 30. The laminate according to claim 5, wherein a molar ratio of2,6-naphthalene group and phenylene group (2,6-naphthalenegroup/phenylene group) of the resin forming the skin layer is 30/70 to92/8.
 31. The laminate according to claim 6, wherein a molar ratio of2,6-naphthalene group and phenylene group (2,6-naphthalenegroup/phenylene group) of the resin forming the skin layer is 30/70 to92/8.
 32. The laminate according to claim 7, wherein a molar ratio of2,6-naphthalene group and phenylene group (2,6-naphthalenegroup/phenylene group) of the resin forming the skin layer is 30/70 to92/8.
 33. The laminate according to claim 8, wherein a molar ratio of2,6-naphthalene group and phenylene group (2,6-naphthalenegroup/phenylene group) of the resin forming the skin layer is 30/70 to92/8.
 34. The laminate according to claim 9, wherein a molar ratio of2,6-naphthalene group and phenylene group (2,6-naphthalenegroup/phenylene group) of the resin forming the skin layer is 30/70 to92/8.
 35. The laminate according to claim 3, wherein the polymer alloyof the heat-resistant resin and the thermoplastic polymer resin is apolymer alloy of a polyarylate resin and polyethylene terephthalate. 36.The laminate according to claim 6, wherein the polymer alloy of theheat-resistant resin and the thermoplastic polymer resin is a polymeralloy of a polyarylate resin and polyethylene terephthalate.